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Journal ArticleDOI

New ligands double the scope of the catalytic asymmetric dihydroxylation of olefins

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TLDR
Improved ligands render terminal olefins good substrates for the osmium-catalyzed asymmetric dihydroxylation (ADH) process as discussed by the authors.
Abstract
Improved ligands render terminal olefins good substrates for the osmium-catalyzed asymmetric dihydroxylation (ADH) process, and the amounts of chiral ligand and osmium catalyst required diminish dramatically

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Book ChapterDOI

9.29 – Enantioselective Synthesis

A. Nova
TL;DR: In this article, the main part of the contribution consists of the presentation of the results obtained by different authors on the computational study of enantioselective catalysis, which have an important practical impact, but the main reason for their selection has been the diversity of problems and methods.
Patent

Ligands chiraux heterocycliques et procede de dihydroxylation asymetrique et catalytique d'olefines

TL;DR: On decrit des procedes d'addition sur une olefine, consistant a effectuer une catalyse par osmium as mentioned in this paper, le procede de dihydroxylation asymetrique de la presente invention, une ollfine, un ligand chiral, un solvant organique, de l'eau, un oxydant, and un compose contenant of l'osmium sont combines.
Journal ArticleDOI

Sharpless Asymmetric Dihydroxylation: An Impressive Gadget for the Synthesis of Natural Products: A Review

TL;DR: Sharpless asymmetric dihydroxylation is an important reaction in the enantioselective synthesis of chiral vicinal diols that involves the treatment of alkene with osmium tetroxide along with optically active quinine ligand as discussed by the authors .
References
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PatentDOI

First practical method for asymmetric epoxidation

TL;DR: In this article, a metal alkoxide is used as a catalyst, where the metal has a coordination number of at least four, and at least one, usually two, of the alkoxide groups bonded to the metal are bonded to asymmetric carbon atoms.
Journal ArticleDOI

Asymmetric dihydroxylation via ligand-accelerated catalysis

TL;DR: Dihydroxylation asymetrique de composes ethyleniques du type styrene, vinylcyclohexane, hexene-3 en les glycols correspondants as mentioned in this paper.
Journal ArticleDOI

An improved synthesis of the taxol side chain and of RP 56976

TL;DR: In this paper, the methode presentee se fait au depart de phenyl-3 dihydroxy-2,3 propionate de methyle via epoxydation, et d'azoture de sodium.
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